Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104353Generated: November 1, 2026

Water → rac-tert-butyl N-((1R,2R)-2-aminocyclopentyl)carbamate

https://huagongshe.com/reaction/2104353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantCyclopentane-1,2-diamineHCID 243938—
SolventDichloromethaneHCID 6344—
Productrac-tert-butyl N-((1R,2R)-2-aminocyclopentyl)carbamateHCID 1704021798.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(±)-trans-1,2-Cyclopentanediamine (WO98/30574) (692 mg) was dissolved in methylene chloride (10 mL), and to the solution were added triethylamine (1.1 mL) and 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (493 mg) at 0° C., followed by stirring at 0° C. for 1 hour. Subsequently, additional 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (493 mg) was added thereto, and the thus-obtained mixture was stirred at room temperature for 7 hours. Water was added to the reaction mixture to partition the mixture. The organic layer was washed with saturated brine, and was dried over sodium sulfate anhydrate. The residue was purified by silica gel flash column chromatography (methylene chloride:methanol=9:1), to thereby give the title compound (395 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576135B2
Source datasetuspto-grants-2009_08
ORD IDord-bebed518f25a460696381fb45085a585
Source noteuspto-grants-2009_08